Canonical Allele Identifier: CA353673381

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93624636T>C (hg19) ; chr3:g.93905792T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905792T>C , CM000665.2:g.93905792T>C	GRCh38
NC_000003.11:g.93624636T>C , CM000665.1:g.93624636T>C	GRCh37
NC_000003.10:g.95107326T>C	NCBI36
NG_009813.1:g.73299A>G , LRG_572:g.73299A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.593A>G	ENSP00000330021.7:p.Asp198Gly
ENST00000394236.9:c.593A>G MANE Select	ENSP00000377783.3:p.Asp198Gly
ENST00000407433.6:c.556+37A>G	ENSP00000385794.2:n.556+37A>G
ENST00000647936.1:c.593A>G	ENSP00000496822.1:p.Asp198Gly
ENST00000648381.1:n.761A>G
ENST00000648853.1:c.551A>G	ENSP00000497262.1:p.Asp184Gly
ENST00000649103.1:c.692A>G	ENSP00000497962.1:n.692A>G
ENST00000650591.1:c.689A>G	ENSP00000497376.1:p.Asp230Gly
ENST00000348974.4:c.689A>G	ENSP00000330021.6:p.Asp230Gly
ENST00000394236.7:c.593A>G	ENSP00000377783.3:p.Asp198Gly
ENST00000407433.5:c.200A>G	ENSP00000385794.1:p.Asp67Gly
NM_000313.3:c.593A>G , LRG_572t1:c.593A>G	NP_000304.2:p.Asp198Gly
NM_001314077.1:c.689A>G , LRG_572t2:c.689A>G	NP_001301006.1:p.Asp230Gly
NM_000313.4:c.593A>G MANE Select	NP_000304.2:p.Asp198Gly
NM_001314077.2:c.689A>G	NP_001301006.1:p.Asp230Gly